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Evolution of competence and DNA uptake specificity in the Pasteurellaceae

BACKGROUND: Many bacteria can take up DNA, but the evolutionary history and function of natural competence and transformation remain obscure. The sporadic distribution of competence suggests it is frequently lost and/or gained, but this has not been examined in an explicitly phylogenetic context. Ad...

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Autores principales: Redfield, Rosemary J, Findlay, Wendy A, Bossé, Janine, Kroll, J Simon, Cameron, Andrew DS, Nash, John HE
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626085/
https://www.ncbi.nlm.nih.gov/pubmed/17038178
http://dx.doi.org/10.1186/1471-2148-6-82
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author Redfield, Rosemary J
Findlay, Wendy A
Bossé, Janine
Kroll, J Simon
Cameron, Andrew DS
Nash, John HE
author_facet Redfield, Rosemary J
Findlay, Wendy A
Bossé, Janine
Kroll, J Simon
Cameron, Andrew DS
Nash, John HE
author_sort Redfield, Rosemary J
collection PubMed
description BACKGROUND: Many bacteria can take up DNA, but the evolutionary history and function of natural competence and transformation remain obscure. The sporadic distribution of competence suggests it is frequently lost and/or gained, but this has not been examined in an explicitly phylogenetic context. Additional insight may come from the sequence specificity of uptake by species such as Haemophilus influenzae, where a 9 bp uptake signal sequence (USS) repeat is both highly overrepresented in the genome and needed for efficient DNA uptake. We used the distribution of competence genes and DNA uptake specificity in H. influenzae's family, the Pasteurellaceae, to examine the ancestry of competence. RESULTS: A phylogeny of the Pasteurellaceae based on 12 protein coding genes from species with sequenced genomes shows two strongly supported subclades: the Hin subclade (H. influenzae, Actinobacillus actinomycetemcomitans, Pasteurella multocida, Mannheimia succiniciproducens, and H. somnus), and the Apl subclade (A. pleuropneumoniae, M. haemolytica, and H. ducreyi). All species contained homologues of all known H. influenzae competence genes, consistent with an ancestral origin of competence. Competence gene defects were identified in three species (H. somnus, H. ducreyi and M. haemolytica); each appeared to be of recent origin. The assumption that USS arise by mutation rather than copying was first confirmed using alignments of H. influenzae proteins with distant homologues. Abundant USS-like repeats were found in all eight Pasteurellacean genomes; the repeat consensuses of species in the Hin subclade were identical to that of H. influenzae (AAGTGCGGT), whereas members of the Apl subclade shared the consensus ACAAGCGGT. All species' USSs had the strong consensus and flanking AT-rich repeats of H. influenzae USSs. DNA uptake and competition experiments demonstrated that the Apl-type repeat is a true USS distinct from the Hin-type USS: A. pleuropneumoniae preferentially takes up DNA fragments containing the Apl-type USS over both H. influenzae and unrelated DNAs, and H. influenzae prefers its own USS over the Apl type. CONCLUSION: Competence and DNA uptake specificity are ancestral properties of the Pasteurellaceae, with divergent USSs and uptake specificity distinguishing only the two major subclades. The conservation of most competence genes over the ~350 million year history of the family suggests that lineages that lose competence may be evolutionary dead ends.
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spelling pubmed-16260852006-10-27 Evolution of competence and DNA uptake specificity in the Pasteurellaceae Redfield, Rosemary J Findlay, Wendy A Bossé, Janine Kroll, J Simon Cameron, Andrew DS Nash, John HE BMC Evol Biol Research Article BACKGROUND: Many bacteria can take up DNA, but the evolutionary history and function of natural competence and transformation remain obscure. The sporadic distribution of competence suggests it is frequently lost and/or gained, but this has not been examined in an explicitly phylogenetic context. Additional insight may come from the sequence specificity of uptake by species such as Haemophilus influenzae, where a 9 bp uptake signal sequence (USS) repeat is both highly overrepresented in the genome and needed for efficient DNA uptake. We used the distribution of competence genes and DNA uptake specificity in H. influenzae's family, the Pasteurellaceae, to examine the ancestry of competence. RESULTS: A phylogeny of the Pasteurellaceae based on 12 protein coding genes from species with sequenced genomes shows two strongly supported subclades: the Hin subclade (H. influenzae, Actinobacillus actinomycetemcomitans, Pasteurella multocida, Mannheimia succiniciproducens, and H. somnus), and the Apl subclade (A. pleuropneumoniae, M. haemolytica, and H. ducreyi). All species contained homologues of all known H. influenzae competence genes, consistent with an ancestral origin of competence. Competence gene defects were identified in three species (H. somnus, H. ducreyi and M. haemolytica); each appeared to be of recent origin. The assumption that USS arise by mutation rather than copying was first confirmed using alignments of H. influenzae proteins with distant homologues. Abundant USS-like repeats were found in all eight Pasteurellacean genomes; the repeat consensuses of species in the Hin subclade were identical to that of H. influenzae (AAGTGCGGT), whereas members of the Apl subclade shared the consensus ACAAGCGGT. All species' USSs had the strong consensus and flanking AT-rich repeats of H. influenzae USSs. DNA uptake and competition experiments demonstrated that the Apl-type repeat is a true USS distinct from the Hin-type USS: A. pleuropneumoniae preferentially takes up DNA fragments containing the Apl-type USS over both H. influenzae and unrelated DNAs, and H. influenzae prefers its own USS over the Apl type. CONCLUSION: Competence and DNA uptake specificity are ancestral properties of the Pasteurellaceae, with divergent USSs and uptake specificity distinguishing only the two major subclades. The conservation of most competence genes over the ~350 million year history of the family suggests that lineages that lose competence may be evolutionary dead ends. BioMed Central 2006-10-12 /pmc/articles/PMC1626085/ /pubmed/17038178 http://dx.doi.org/10.1186/1471-2148-6-82 Text en Copyright © 2006 Redfield et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Redfield, Rosemary J
Findlay, Wendy A
Bossé, Janine
Kroll, J Simon
Cameron, Andrew DS
Nash, John HE
Evolution of competence and DNA uptake specificity in the Pasteurellaceae
title Evolution of competence and DNA uptake specificity in the Pasteurellaceae
title_full Evolution of competence and DNA uptake specificity in the Pasteurellaceae
title_fullStr Evolution of competence and DNA uptake specificity in the Pasteurellaceae
title_full_unstemmed Evolution of competence and DNA uptake specificity in the Pasteurellaceae
title_short Evolution of competence and DNA uptake specificity in the Pasteurellaceae
title_sort evolution of competence and dna uptake specificity in the pasteurellaceae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626085/
https://www.ncbi.nlm.nih.gov/pubmed/17038178
http://dx.doi.org/10.1186/1471-2148-6-82
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